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American Journal of Human Genetics
|
October 1, 1994
Genetic mapping of a locus for multiple epiphyseal dysplasia (EDM2) to a region of chromosome 1 containing a type IX collagen gene
M D Briggs, H Choi, M L Warman, et al.
American Journal of Human Genetics
|
June 19, 1998
Genetic heterogeneity of Saethre-Chotzen syndrome, due to TWIST and FGFR mutations
W A Paznekas, M L Cunningham, T D Howard, et al.
Human Mutation
|
January 22, 2008
Clinical and molecular features of mitochondrial DNA depletion due to mutations in deoxyguanosine kinase
D P Dimmock, Q Zhang, C Dionisi-Vici, et al.
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Search research articles
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Showing results (11-20 of 13) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 13 results.
American Journal of Human Genetics
|
October 1, 1994
Genetic mapping of a locus for multiple epiphyseal dysplasia (EDM2) to a region of chromosome 1 containing a type IX collagen gene
M D Briggs, H Choi, M L Warman, et al.
American Journal of Human Genetics
|
June 19, 1998
Genetic heterogeneity of Saethre-Chotzen syndrome, due to TWIST and FGFR mutations
W A Paznekas, M L Cunningham, T D Howard, et al.
Human Mutation
|
January 22, 2008
Clinical and molecular features of mitochondrial DNA depletion due to mutations in deoxyguanosine kinase
D P Dimmock, Q Zhang, C Dionisi-Vici, et al.
Page
of 2